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Summary Literature (0)
MIM:614501 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, CRANIOFACIAL ABNORMALITIES, AND SEIZURES; NEDHCS

Xenbase Genes: snip1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013787 - psychomotor retardation, epilepsy, and craniofacial dysmorphism